SCHEMBL422832

SCHEMBL422832

COc1cccc(C[O])c1F

nearest known ligand 0.44

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HTR2A P28223 1/20 0.44
HTR2C P28335 1/20 0.44
IDO1 P14902 3/20 0.41
TAAR1 Q96RJ0 1/20 0.41
L3MBTL1 Q9Y468 2/20 0.41
CA12 O43570 2/20 0.41
CA1 P00915 2/20 0.41
CA2 P00918 2/20 0.41
CA7 P43166 2/20 0.41
CA9 Q16790 2/20 0.41
CA14 Q9ULX7 2/20 0.41
CA4 P22748 1/20 0.41
SMN1; SMN2 Q16637 2/20 0.40
CHRM2 P08172 1/20 0.40
CHRM1 P11229 1/20 0.40
ALKBH1 Q13686 1/20 0.40
HTT P42858 1/20 0.40
ALDH1A1 P00352 1/20 0.39
GAA P10253 1/20 0.39
MAPT P10636 1/20 0.39

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
SCHEMBL172225 0.90 HTR2A (0.46) HTR2AHTR2CIDO1TAAR1L3MBTL1
SCHEMBL8926 0.82 TAAR1 (0.52) HTR2AHTR2CIDO1TAAR1L3MBTL1
SCHEMBL29792655 0.82 TAAR1 (0.52) HTR2AHTR2CIDO1TAAR1L3MBTL1
SCHEMBL3533385 0.80 HTR2A (0.44) HTR2AHTR2CIDO1TAAR1L3MBTL1
SCHEMBL17351757 0.80 IDO1 (0.46) HTR2AHTR2CIDO1TAAR1L3MBTL1
SCHEMBL489675 0.80 HTR2A (0.44) HTR2AHTR2CIDO1TAAR1L3MBTL1
Bromide SCHEMBL15741709 0.80 TAAR1 (0.50) HTR2AHTR2CIDO1TAAR1L3MBTL1
SCHEMBL489913 0.80 HTR2A (0.48) HTR2AHTR2CIDO1TAAR1L3MBTL1
SCHEMBL29835952 0.80 HTR2A (0.44) HTR2AHTR2CIDO1TAAR1L3MBTL1
SCHEMBL29783095 0.80 HTR2A (0.48) HTR2AHTR2CIDO1TAAR1L3MBTL1

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 32 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3456721-B1 METHOD OF PRODUCING COMPOUNDS HAVING HIV INTEGRASE INHIVITORY ACTIVITY SHIONOGI & CO (JP) 2021-02-24 EP disclosed
EP-3456721-A2 METHOD OF PRODUCING COMPOUNDS HAVING HIV INTEGRASE INHIVITORY ACTIVITY Shionogi & Co., Ltd (JP) 2019-03-20 EP disclosed
EP-3127908-B1 PROCESS FOR PREPARING COMPOUND HAVING HIV INTEGRASE INHIBITORY ACTIVITY SHIONOGI & CO (JP) 2018-11-28 EP disclosed
US-10125146-B2 Crystalline methyl (4R,12aS)-7-(benzyloxy)-4-methyl-6,8-dioxo-3,4,6,8,12,12a-hexahydro-2H-pyrido[1′,2′:4,5]pyrazino[2,1-b][1,3]oxazine-9-carboxylate SHIONOGI & CO., LTD. (JP) 2018-11-13 US disclosed
US-10125147-B2 Crystalline methyl (4R,12aS)-7-(benzyloxy)-4-methyl-6,8-dioxo-3,4,6,8,12,12a-hexahydro-2H-pyrido[1′,2′:4,5]pyrazino[2,1-b][1,3]oxazine-9-carboxylate SHIONOGI & CO., LTD. (JP) 2018-11-13 US disclosed
US-10000508-B2 Crystalline dimethyl 3-(benzyloxy)-1-(2,2-dimethoxyethyl)-4-oxo-1,4-dihydropyridine-2,5-dicarboxylate SHIONOGI & CO., LTD (JP) 2018-06-19 US disclosed
US-9969750-B2 Method of producing (3S,11aR)-6,8-dihalo-3-methyl-2,3,11,11a-tetrahydrooxazolo[3,2-a]pyrido[1,2-d]pyrazine-5,7-diones SHIONOGI AND CO., LTD. (JP) 2018-05-15 US disclosed
US-20180044351-A1 METHODS OF PRODUCING COMPOUNDS HAVING HIV INTEGRASE INHIBITORY ACTIVITY SHIONOGI & CO., LTD. (JP) 2018-02-15 US disclosed
US-20180037593-A1 METHODS OF PRODUCING COMPOUNDS HAVING HIV INTEGRASE INHIBITORY ACTIVITY SHIONOGI & CO., LTD. (JP) 2018-02-08 US disclosed
US-20180037591-A1 METHODS OF PRODUCING COMPOUNDS HAVING HIV INTEGRASE INHIBITORY ACTIVITY SHIONOGI & CO., LTD. (JP) 2018-02-08 US disclosed
US-20160002211-A1 METHOD OF PRODUCING PYRONE AND PYRIDONE DERIVATIVES SHIONOGI & CO., LTD. (JP) 2016-01-07 US disclosed
US-20150038702-A1 Method of producing compounds having HIV integrase inhivitory activity SHINOGI & CO., LTD. (JP) 2015-02-05 US disclosed
US-20150031876-A1 METHOD FOR PRODUCING PYRONE AND PYRIDONE DERIVATIVES SHIONOGI & CO., LTD. (JP) 2015-01-29 US disclosed
US-8865907-B2 Method of producing pyrone and pyridone derivatives SHIONOGI & CO., LTD. (JP) 2014-10-21 US disclosed
US-20140011995-A1 Process for Preparing Compound Having HIV Integrase Inhibitory Activity SHINOGI & CO., LTD (JP) 2014-01-09 US disclosed
EP-2602260-A1 PROCESS FOR PREPARING COMPOUND HAVING HIV INTEGRASE INHIBITORY ACTIVITY Shionogi&Co., Ltd. (JP) 2013-06-12 EP disclosed
EP-2412709-A1 PROCESS FOR PRODUCING PYRONE AND PYRIDONE DERIVATIVES Shionogi & Co., Ltd. (JP) 2012-02-01 EP disclosed
US-20120022251-A1 METHOD OF PRODUCING PYRONE AND PYRIDONE DERIVATIVES SHIONOGI & CO., LTD. (JP) 2012-01-26 US disclosed
US-6476021-B1 Compounds having cGMP-PDE inhibitory effect MOCHIDA PHARMACEUTICAL CO., LTD. (JP) 2002-11-05 US disclosed
EP-1048666-A1 NOVEL COMPOUNDS HAVING cGMP-PDE INHIBITORY EFFECT MOCHIDA PHARMACEUTICAL CO., LTD. (JP) 2000-11-02 EP disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (11 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-10125146-B2 Crystalline methyl (4R,12aS)-7-(benzyloxy)-4-methyl-6,8-dioxo-3,4,6,8,12,12a-hexahydro-2H-pyrido[1′,2′:4,5]pyrazino[2,1-b][1,3]oxazine-9-carboxylate H1-4, CYP4Z1, H1-2 HTR2A 178/4885HTR2C 128/4885IDO1 1386/4885
US-20150038702-A1 Method of producing compounds having HIV integrase inhivitory activity XDH, IMPDH1, IMPA1 HTR2A 3205/4885HTR2C 2519/4885IDO1 42/4885
US-10125147-B2 Crystalline methyl (4R,12aS)-7-(benzyloxy)-4-methyl-6,8-dioxo-3,4,6,8,12,12a-hexahydro-2H-pyrido[1′,2′:4,5]pyrazino[2,1-b][1,3]oxazine-9-carboxylate PYM1, DRD4, MBD2 HTR2A 302/4885HTR2C 128/4885IDO1 730/4885
US-20150031876-A1 METHOD FOR PRODUCING PYRONE AND PYRIDONE DERIVATIVES PNPO, PDXK, CYP3A5 HTR2A 1536/4885HTR2C 1662/4885IDO1 33/4885
US-20120022251-A1 METHOD OF PRODUCING PYRONE AND PYRIDONE DERIVATIVES PNPO, PDXK, CYP3A5 HTR2A 1427/4885HTR2C 1594/4885IDO1 25/4885
US-20180044351-A1 METHODS OF PRODUCING COMPOUNDS HAVING HIV INTEGRASE INHIBITORY ACTIVITY CYP3A4, DRD4, CCND2 HTR2A 3022/4885HTR2C 1871/4885IDO1 230/4885
US-10000508-B2 Crystalline dimethyl 3-(benzyloxy)-1-(2,2-dimethoxyethyl)-4-oxo-1,4-dihydropyridine-2,5-dicarboxylate DPYD, ODC1, PKD1 HTR2A 1553/4885HTR2C 851/4885IDO1 1006/4885
US-20140011995-A1 Process for Preparing Compound Having HIV Integrase Inhibitory Activity DRD4, XDH, CCND2 HTR2A 3060/4885HTR2C 2007/4885IDO1 189/4885
US-20180037593-A1 METHODS OF PRODUCING COMPOUNDS HAVING HIV INTEGRASE INHIBITORY ACTIVITY XDH, DRD4, PYM1 HTR2A 2840/4885HTR2C 1791/4885IDO1 135/4885
US-20160002211-A1 METHOD OF PRODUCING PYRONE AND PYRIDONE DERIVATIVES PNPO, PDXK, CYP3A5 HTR2A 1427/4885HTR2C 1594/4885IDO1 25/4885
US-20180037591-A1 METHODS OF PRODUCING COMPOUNDS HAVING HIV INTEGRASE INHIBITORY ACTIVITY XDH, DRD4, PYM1 HTR2A 2840/4885HTR2C 1791/4885IDO1 135/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.